Addition reactions to chiral aziridine-2-carboxaldimine toward various enantiopure nitrogen-containing heterocycles
Chiral (2R,1′R)-(1′-phenylethyl)aziridine-2-carboxaldimine was utilized as a nitrogen-containing starting substrate for the preparation of various enantiopure nitrogen-containing heterocycles. The additions of nucleophiles including organomagnesium reagen
Noh, Heui-Yoon,Kim, Sang-Woo,Seong, In Paek,Ha, Hyun-Joon,Yun, Hoseop,Won, Koo Lee
p. 9281 - 9290
(2007/10/03)
Highly Stereoselective Addition of Organomagnesium Reagents to Aziridinyl-2-carboxaldimine: Preparation of Enantiopure 2-Aminomethylaziridines and 4,5-Disubstituted Imidazolidin-2-ones
The addition of alkyl- and arylmagnesium reagents to chiral [1′(R)-α-methylbenzyl]aziridine-2(R)-carboxaldimines was carried out in a highly stereoselective manner to give 2-aminomethylaziridine. Further treatment of 2-aminomethylaziridines with triphosge
Suh, Man-Jin,Kim, Sang Woo,Beak, Seong In,Ha, Hyun-Joon,Lee, Won Koo
p. 489 - 492
(2007/10/03)
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